{{Rsnum
|rsid=137853325
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=IKBKG
|position=154564450
|Gene_s=IKBKG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300248
|variant=0009
|rsnum=137853325
}}{{ClinVar
|rsid=137853325
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=153792665
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=IKBKG:8517
|GENE_NAME=IKBKG
|GENE_ID=8517
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153792665T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300248.0009
|CLNSIG=5
|CLNCUI=C1846006
|CLNDBN=Hypohidrotic ectodermal dysplasia with immune deficiency; HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH HYPOHIDROTIC ECTODERMAL DYSPLASIA
|Disease=Hypohidrotic ectodermal dysplasia with immune deficiency; HYPER-IgM IMMUNODEFICIENCY
|CLNACC=RCV000012207.10; RCV000012208.10
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1846006:300291:238468:98813
}}